Fluorinative ring-expansion of cyclic ethers using p-iodotoluene difluoride. Stereoselective synthesis of fluoro cyclic ethers
โ Scribed by Tomotake Inagaki; Yutaka Nakamura; Masanori Sawaguchi; Norihiko Yoneda; Shinichi Ayuba; Shoji Hara
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 213 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Fluorinated five-to seven-membered cyclic ethers were stereoselectively synthesized from four-to six-membered cyclic ethers having an iodoalkyl substituent by fluorinative ring-expansion reaction using p-iodotoluene difluoride.
๐ SIMILAR VOLUMES
Fluoriuative ring-contraction of cyclic alkenes is induced by iodotoluene difluctide and Et3N-5HF to give difluoro cycioalkanes selectively.
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